All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00892 FIH hypoparathyroidism, familial isolated (FIH) 146200 0 0 GCM2, PTH - autosomal dominant